Title: Florida Entomologist
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Permanent Link: http://ufdc.ufl.edu/UF00098813/00258
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Title: Florida Entomologist
Physical Description: Serial
Creator: Florida Entomological Society
Publisher: Florida Entomological Society
Place of Publication: Winter Haven, Fla.
Publication Date: 1942
Copyright Date: 1917
Subject: Florida Entomological Society
Entomology -- Periodicals
Insects -- Florida
Insects -- Florida -- Periodicals
Insects -- Periodicals
General Note: Eigenfactor: Florida Entomologist: http://www.bioone.org/doi/full/10.1653/024.092.0401
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Bibliographic ID: UF00098813
Volume ID: VID00258
Source Institution: University of Florida
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Florida Entomologist
Official Organ of the Florida Entomological Society

VOL. XXV OCTOBER, 1942 No. 3

Anisomorpha buprestoides Stoll.*

The Florida walking stick Anisomorpha buprestoides Stoll.
is a lubberly Phasmid occurring in considerable numbers in the
state of Florida. An acrid fluid elaborated by the thoracic re-
pellent glands can be ejected 10-18 inches in a fine mist by both
sexes and the insect is often called the "musk mare."
This insect is herbivorous, deliberate in nature, and depend-
ent upon its mimetic form and repellent fluid for protection.
It is gregarious at mating time, large numbers of males and
females in coitu clinging beneath fronds of scrub palmettoes in
late summer and fall. The black seed-like eggs are dropped to
the ground and hatch during the following spring, or remain
until the second spring before hatching.

The Florida walking stick is a North American insect, occur-
ring in the Southeastern States from Mississippi to the southern
tip of Florida, and as far north as South Carolina. A. ferruginea
is a smiliar insect found farther northward. It is a slightly
smaller member of the genus, and lacks the conspicuous mark-
ings of buprestoides. Specimens used for this study were col-
lected at Gainesville, Fla., in October 1933 and 1934.

A. buprestoides is elongate and subcylindrical, wingless, and furnished
with slender legs and long, filiform antennae. The female is robust, aver-
aging about 6.77 cm. in length and 0.90 cm. in width at the posterior margin
of the metathorax. The male is small, the average length being 4.17 cm.
Condensed from a thesis presented in 1935 in partial fulfilment of the
requirements for the degree of Master of Science in the Graduate School
of the University of Florida.


and the width 0.42 cm. For comparison the male and female are drawn
to the same scale in the figures.
The general body color is various shades of reddish or grayish brown,
often fuscous. There are longitudinal black stripes, one dorsal and two
subdorsal, separated by two yellow or gray addorsal stripes which also
extend the full length of the insect.

The head (Figs. 1-4) is subquadrate, nearly oval in shape, flattened
dorsally and ventrally, the gena (Fig. 3 GE) wide. The facial aspect is
directed cephalad in the nymph as well as in the adult. The stem of the
epicranial suture (Fig. 1 ES) is a faint line extending cephalad from the
occiput (Fig. 3 OC) to a point between the antennal sclerites (ANS).
Two addorsal lateral sutures (LS) originate at a granule at the inner
margin of each eye (Fig. 1 GR, E) and extend caudad to the postoccipital
suture (Fig. 3 POC). The frontogenal sutures (Fig. 1 FGS) are short,
terminating near the cephalic margins of the eyes. These sutures are con-
sidered as the cephalic portions of the epicranial arms which have been
isolated from the epicranial suture by encroachment of the antennal scler-
ites.' The vertex (Fig. 1 VX) includes about one-third of the head surface.
The occiput, or posterior portion of the epicranium, is not set off by a
suture. The latero-ventral portions of the occipital area are termed the
postgenae (Fig. 4 PGE). The subgenal suture (SGS) forms an internal
ridge strengthening the latero-ventral edges of the cranium. The fronto-
clypeal suture (Fig. 2 FCS) unites the ends of the subgenal sutures. The
frons, or face (FR), is a small, unpaired, median sclerite. The clypeus
(CLP) is articulated to the frons along the fronto-clypeal or epistomal
suture, and is capable of restricted motion.
The antennae (Fig. 5) are inserted in circular membranes (MB) giving
some freedom of motion, although their general position is in a horizontal
line extending forward from the head. They are over two-thirds the body
length, averaging about 4.20 cm. for the female and 3.56 cm. for the male.
There are 25-27 segments in the antennae of the female and 22-24 for the
The compound eyes are prominent (Fig. 1 E), and are set off by ocular
sclerites (OS). No ocelli, or simple eyes, are present.
The bilobed and deeply cleft labrum, or upper lip (Fig. 2 LM), is sus-
pended from the clypeus along the clypeo-labral suture (CLS), and is moved
by muscles inserted in its base. The mandibles (Figs. 2, 3 MD and Fig. 6)
are large and heavily sclerotized, moving freely inward and outward be-
tween the anterior and posterior articulations (Figs. 2, 6 C, A). The
basimandible (Fig. 3 BMD) is a narrow plate by which the mandible is
articulated to the gena along the mandibular suture. The hypopharynx
(Fig. 3 HY and Fig. 7) hangs like a tongue in the preoral cavity. The
maxillae (Figs. 2, 4 MX) are typical of the Orthoptera in structure, con-
sisting of a cardo, stipes, galea, lacinia, palpifer, and palpus. The dis-
tagalea (Figs. 8, 9 DG) overlaps the distal portion of the lacinia (LA)
as in other phasmids; is hood-shaped, pubescent, bearing a pointed lobular

1 YUASA, HACHIRO, 1920. The anatomy of the head and mouthparts of
Orthoptera and Euplexoptera. Jour. Morph., 33: No. 2, March, 1920.

VOL. XXV-No. 3 35

process, the galealobulus (GL). The lacinia is flattened, heavily sclerotized,
and separated from the stipes (ST) by a distinct suture. The lacinia bears
two laciniadentes (LD) whose function is apparently that of holding food.
The labium, or lower lip (Fig. 10), is attached to the ventral portion of
the head by means of the cervical membrane (Fig. 4 CV), no cula being
present. The labium is articulated laterally to the anterior extremities of
the postocciput (Fig. 3 POC). Note the small size of the male labium
(Fig. 11).
The neck, or cervicum (Fig. 3 CV) is not visible from the dorsal aspect
as the pronotum covers the occipital portion of the head. The cervical
sclerites (LC) are articulated to the precostal bridge (ACX) of the thorax
(1 TH) and extend to the postocciput (POC). The two pairs of sclerites
are so closely articulated as to seem one pair of plates. Crampton 2 refers
to each of these plates as a cervicale.
The thorax of A. buprestoides (Figs. 12-14) is apterous and bears three
pairs of slender legs well suited to the slow, deliberate gait of the insect.
The male thorax is small and slender (Figs. 18-20). The segments are
of nearly the same width, while the second and third segments of the female
thorax are stout. The female thorax is about 2.82 cm. long, ranging from
2.46 cm. to 3.08 cm. in specimens collected at Gainesville, Fla. The male
thorax is about 1.60 cm. long, ranging from 1.43 cm. to 1.84 cm. in length.
The true prothoracic spiracles have been lost, but the second pair has
migrated forward into the conjunctival fold between the prothorax (Fig.
14 1 TH) and metathorax (2 TH) until they appear to be true prothoracic
spiracles (SP 1). One pair (SP 2) is found posterior to the mesothorax.
The first pair of abdominal spiracles (SP 3) has migrated into the meta-
thorax (3 TH) upon the elimination of the first true abdominal segment.
The pronotum (Fig. 12 1N) is small, averaging 0.56 cm. in length in
the female and 0.33 cm. in the male. The latero-cephalic corners of the
pronotum are notched to expose the external openings of the thoracic
repellent glands (Fig. 12 GL), permitting the insect to eject the acrid
fluid in a vertical direction.
The mesonotum (Fig. 12 2N) is distinguished by its length, averaging
about 1.22 cm. in the female and 073 cm. in the male. The ridge in the
costal region (CS) is not as pronounced as in the pronotum. The mesono-
tum has two subdorsal and two lateral rows of granules (GR), noticeable
because of their light color. The anal margin of each thoracic tergite forms
a lightly sclerotized fold or conjunctiva (Figs. 16, 17 CJA) overlapping
the next tergite. It is of interest to note that the ventral plate or sternite
of the mesothorax overlaps both the prothoracic and metathoracic sternites
(S), a condition not found in other intersegmental areas on this insect.
The metanotum of the Florida walking stick averages about 1.04 cm.
in length for the female and 0.63 cm. for the male. The lateral margins
bear vestiges of a division (Figs. 12, 14).

2 CRAMPTON, G. C., 1926. A comparison of the neck and prothoracic
sclerites throughout the orders of insects. Trans. Amer. Ent. Soc. LII,
pp. 199-248, 1926.



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VOL. XXV-No. 3

1-4 Dorsal, cephalic, lateral and ventral aspects of the head of female
Florida walking stick, Anisomorpha buprestoides Stoll. ACX, pre-
costal bridge; ANS, antennal sclerite; ANT, antenna; BMD, basi-
mandible; CLP, clypeus; CLS, clypeo-labral suture; CO, cardo; CV,
cervicum; E, eye; ES, epicranial suture; FCS, fronto-clypeal suture;
FGS, fronto-genal suture; FOR, occipital foramen; FR, frons; GE,
gena; GL, thoracic glandular opening; GR, granule; HY, hypo-
pharynx; LB, labium; LC, cervicale; LM, labrum; LS, lateral suture;
LPLP, labial palpus; MD, mandible; MDS, mandibular suture;
MPLP, maxillary palpus; MX, maxilla; OC, occiput; OS, ocular
sclerite; POC, postocciput; PGE, postgena; PT, posterior tentorial
pit; SGS, subgenal suture; SMT, submentum; STE, setae; Ith, pro-
thorax; VX, vertex.
5 Antenna of the female walking stick. MB, membrane; SC, scape;
STE, setae.
6 Lateral and ental aspect of right mandible. A, posterior articula-
tion; C, anterior articulation.
7 Lateral aspect of hypopharynx of female walking stick.
8-9 Ventral and dorsal aspect of right maxilla. BG, basigalea; CO,
cardo; DG, distagalea; GL, galealobulus; LA, lacinia; LD, lacinia-
dentes; PF, palpifer; PLP, palpus; Q, groove; ST, stipes; STE, setae.
10-11 Ventral aspect of female and male labium, showing proportionate
size. GL, glossa; LIG, ligula; MB, membrane, MT, mentum; PGL,
paraglossa; PLG, palpiger; PLP, palpus; SMT, submentum; STE,
12-14 Dorsal, ventral and lateral aspect of female thorax.
15 Lateral aspect of metathorax of female.
16 Cross section of body wall between meso- and metathorax.
17 Cross section of body wall between metathorax and abdomen.

The prosternum, or ventral wall of the prothorax, is divided into two
plates. The large anterior plate, or eusternum (Fig. 13 1 S) is evident
in the figure. The second plate, or sternellum, is completely hidden by the
anterior margin of the mesosternum (1M).
The mesosternum (Fig. 13 2S) overlaps the prosternum, forming a very
flexible connection. The small anterior plate (1M) is joined to the large
posterior plate (2M) by a lightly sclerotized, crescent-shaped suture, allow-
ing considerable freedom of motion between the prothorax and mesothorax.
The external impressions of the sternal apophyses (AP) are found between
the bases of the coxae. The mesosternum is bounded laterally by the pleuro-
ventral line (A-A).
The metasternum (Fig. 13 3S) is short and broad. The impressions
of the sternal apophyses are present and much deeper than in the meso-
sternum. The posterior margin of this plate is superimposed upon the first
abdominal segment.
The prothoracic pleurite (Fig. 14 1TH) is divided into three sclerites
the precoxal bridge (ACX), episternum (EPS), and epimeron (EPM).
The coxal cavity is large and membranous. The cervicale (Fig. 3 LC)
is articulated to the anterior margin of the precoxal bridge forming an



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VOL. XXV-No. 3 39

articulation between the head and thorax. One pair of spiracles (Fig. 14
SP 1) occurs.
The mesothoracic and metathoracic pleurites are similar in structure
and the latter only will be described. The episternum (Fig. 15 EPS) and
precoxal bridge (ACX) are slender and divided by a suture as in many of
the lower insects, the precoxal bridge constituting a separate sclerite or
anterior laterale. The epimeron (EPM) is separated from the episternum
by the pleural suture (PLS) and forms a bridge from the notum (3N) to
the coxa (CX). The pleural suture forms internally the pleural bridge.
An extension of the epimeron of the metapleurite forms a postcoxal bridge
(PCX), a plate that is not found in the mesopleurite. The trochantin (TN)
is flexible, permitting free motion of the coxa. The second and third pairs
of spiracles (SP2, SP3) are found in the intersegmental areas anterior
and posterior to the metathoracic pleurite. The original first abdominal
spiracle has migrated forward to a position between the epimeron and
notum of the metathorax.
The legs of the Florida walking stick are long and slender, suited to
the deliberate gait of this insect. All three pairs of legs are similar and
the prothoracic leg is illustrated by Fig. 34. The leg consists of a coxa
(CX), trochanter (TR), femur (F), tibia (TB), tarsus (TAR), and a

18-20 Dorsal, ventral and lateral aspect of the male thorax.
21 Cross section of body wall of male between meso- and metathorax.
A-A, dorso-pleural suture; ACX, antecoxal bridge; AP, extenal im-
pressions of sternal apophyses; B-B, pleuro-ventral suture; CJA,
conjunctival fold; CS, costa; CX, coxa; EPM, epimeron; EPS, epi-
sternum; GL, openings of the thoracic repellent glands; GR, granule;
J, submarginal suture of presternum; L1, anterior lip of spiracle;
L2, posterior lip of spiracle; 1M, anterior plate of mesosternum;
2M, posterior plate of mesosternum; MB, membrane; 1N-3N, pro-,
meso-, and metanotum; PC, precosta; PCX, postcoxal bridge; PLS,
pleural suture; PS, presternum; PTR, peritreme; R, lateral ridge
of pronotum; S, sternite; 1S-3S, pro-, meso-, and metasternum;
SP1-SP3, spiracles; 1TH-3TH, pro-, meso-, and metathorax; TN,
trochantin; TR, trochanter.
22-24 Dorsal, ventral, and lateral aspect of male abdomen.
25-27 Dorsal, ventral, and lateral aspect of female abdomen.
28 Ventral aspect of segments 7-10 of female abdomen.
29-30 Lateral and ventral aspect of tip of female abdomen.
31 Longitudinal section of abdominal wall showing intersegmental area.
32-33 Ventral and latero-ventral aspect of tip of male abdomen. A-A,
dorso-pleural suture; AN, anus; B-B, pleuro-ventral suture; CER,
cercus; 8CXX, subgenital plate of female; 9CXX, subgenital plate
of male; EPPT, epiproct; GLP, aedeagus; MB, membrane; PAPT,
paraproct; PC, precosta; 2PL-7PL, second to seventh pleurites; 2S-
10S, second to tenth sternites; SP, spiracle; 2T-10T, second to tenth
tergites; 1VL-3VL, first to third valvulae of ovipositor; 1VLF, first
valvifer; VUL, vulva.
34 Lateral view of prothoracic leg of female.
35 Lateral view of prothoracic tarsus of female. AR, arolium; CX,
coxa; F, femur; PV, pulvilli; STE, setae; TAR, tarsus; TB, tibia;.
UN, ungues or claws.


pretarsus comprising a pair of lateral claws (Fig. 35 UN) and a median
arolium (AR). The first four segments of the tarsus bear ventrally pairs
of pulvilli (PV).
The gravid female walking stick has a very stout abdomen that tapers
gradually from the first to the last segment (Figs. 25-27). The abdomen
of the male is slender, varying little in width (Figs. 22-24). The female
abdomen averages 3.69 cm. in length and the male 2.33 cm. The largest
female collected had an abdomen 4.05 cm. long.
The tergum (Figs. 22, 25) is composed of nine plates, or tergites, each
of which telescopes under the preceding plate. The original first tergite
has become obsolete.
The sternum, or ventral wall, of the abdomen is shown for the male
and female respectively in Figs. 23 and 26. Segment one has become
obsolete in both male and female, so the true second plate is designated
as the second sternite (2S). The female abdomen has sternites two to eight,
while the male has the ninth also. The tenth male sternite has been split,
reduced in size, and displaced to the sides of the segment (Fig. 33 10S).
The tenth female sternite is well developed (Fig. 26 10S) indicating, ac-
cording to Snodgrass 3 a great extent of musculature of the cerci (CER).
An eleventh segment is represented by the paraprocts (Fig. 28 PAPT)
which appear to be lobes of the tenth segment, the suture having been
obliterated. Dorsad to the anus (Fig. 29 AN) is a small supra-anal plate,
or epiproct (EPPT), corresponding to the eleventh tergite in Thysanura.
The Florida walking stick has a distinct lateral abdominal region, or
pleuron, another evidence of the primitiveness of this species. There are
six pairs of pleurites (Fig. 27 2PL-7PL), bounded dorsally by the dorso-
pleural suture (Fig. 26 A-A) and ventrally by the pleuro-ventral suture
(B-B). These sutures permit the abdomen to expand and contract for
breathing. Spiracles are found on segments two to eight. The male
pleurites are very narrow (Fig. 24).

The genitalia are borne in the primitive ventral position. The ovi-
positor of the female (Figs. 29, 30 1VL-3VL) is poorly developed, a condi-
tion typical of the Phasmidae. The vulva (VUL), or genital aperture, is
situated in the eighth abdominal sternite and protected by a prolongation
of the sternite, the subgenital plate (Fig. 28 CXX). Three pairs of pro-
cesses, the gonapophyses or valvulae (1VL-3VL), form the ovipositor. The
first valvulae arise from the posterior margin of the eighth sternum and
consist of the valvifers (1VLF), and the blades (1VL). The second val-
vulae lie in the primitive position within the third valvulae, with which
they are united laterally except for their distal third. The second and
third valvulae arise from the ninth abdominal segment. They are soft
and poorly developed.
The ninth sternite (Fig. 32 9S) in the male is reduced in size and is

3 SNODGRASS,,R. E., 1931. Morphology of the insect abdomen. Part I.
General structure of the abdomen and its appendages. Smithsonian Misc.
Coll. 85: No. 6, 128 pp., 46 figs.

VOL. XXV-No. 3

divided from the subgenital plate, or hypandrium (9CXX), by a suture.
This division affords the subgenital plate freedom of motion to permit
copulation. The copulatory organ, or aedeagus (Fig. 33 GLP) is an irreg-
ularly shaped mass of erectile tissue. In the act of copulation this organ
is typically inserted into the vulva, as many specimens were collected in
this position. Nevertheless several males and females were collected with
the male organ inserted in a midventral opening posterior to the seventh
female sternite (Fig. 28) which is possibly a primitive gonopore.

The writer wishes to express his appreciation to Dr. J. T. Creighton,
his faculty advisor, for assistance in this investigation. This work was
completed in the Department of Entomology, College of Agriculture, Uni-
versity of Florida, before entering the Federal service.
Nematode Laboratory, White-Fringed Beetle Control
Gulfport, Miss., Sptember 5, 1942

(Continued from last issue)
F. M. Webster worked on the buffalo gnats of the southern
Mississippi valley and his report on these pests has been the
standard for years. It has been told that a resident of Arkansas
said that the Government sent a man down there to work on
the buffalo gnats but he "did not do a damn thing but put a
few in a bottle."
F. W. Mally began his southern career under Professor Riley,
working first in Louisiana, but his extended career in Texas
included positions as Professor of Entomology in the Agricul-
tural College, State Entomologist, Entomologist of the Experi-
ment Station and in later years as a County Agent.
Howard E. Weed, Entomologist with the Mississippi Agri-
cultural College, was a successful collector and supplied speci-
mens for description by many specialists.

C. H. Fernald may be mentioned here because of the fact
that he trained many entomologists who took positions in south-
ern states and consequently acquired a distinct influence on the
development of entomology in this region.
H. A. Morgan, who was honored guest two years ago for
the Entomological Conference, began with a successful career
in Louisiana over fifty years ago, later holding a position of


Entomologist, Station Director and President of University of
Tennessee and lately a member of the T. V. A.
P. H. Rolfs began work as an entomologist in Florida in
1891 but was also botanist and later director of the Station and
still later President of the Agriculture College of Minas Geraes,
H. A. Gossard was entomologist of the Experiment Station
when it was located at Lake City, later he accepted a position
at Ohio Experiment Station which he occupied until his death.
F. L. Harvey served as botanist and entomologist in the
Agricultural College of Arkansas but later went to Maine.
H. E. Summers was entomologist of the Experiment Station
in Tennessee for a few years, later worked with Professor Forbes
in Illinois and then as entomologist in Iowa.
E. D. Sanderson served for a number of years as Entomolo-
gist of the Agricultural College in Texas, later in New Hamp-
shire and more recently turned to the field of rural sociology.
E. W. Berger began his long career as entomologist in the
Experiment Station and State Plant Board in 1906.
Wilmon Newell served as entomologist in Louisiana, Texas
and Georgia, coming to Florida in 1915 to head the work in
the State Plant Board and serving also as Director of Experi-
ment Station, Dean of Agriculture and Provost in Agriculture.
E. D. Ball worked for several years on the celery insects
at Sanford, but his career has covered positions in Iowa, Colo-
rado, Utah, Wisconsin and Arizona.
W. J. Hunter for many years was in charge of cotton insect
C. W. Stiles spent a number of years in the South and while
his work was mainly devoted to public health matters, his con-
nection with the International Commission of Nomenclature
included entomological problems.
R. W. Harned, at present in charge of the Division of Cotton
Insects in Washington, was for many years the head of the
entomological work in Mississippi.
G. W. Herrick, Emeritus Professor at Cornell University,
was the Professor of Entomology at the Mississippi Agricultural
College from 1897 to 1908 and entomologist of Texas A. & M.

Official Organ of the Florida Entomological Society
Gainesville, Florida

VOL. XXV OCTOBER, 1942 No. 3

J. R. WATSON, Gainesville..---. --.....--................--.. ..-................Editor
E. W. BERGER, Gainesville -----. ------- -----Associate Editor
C. B. WISECUP, Box 309, Plant City -....-..-.........- Business Manager
Issued once every three months. Free to all members of the
Subscription price to non-members is $1.00 per year in ad-
vance; 35 cents per copy.


Frankliniella tolucensis sp. nov.
FEMALE: Color almost a uniform brown (Raw umber, Ridgeway's color
standards); head and femora a little lighter brown; tarsi pale yellow;
antennal segment III pale brownish yellow in basal half (except pedicel)
shaded with light brown in apical half, concolorous with basal half of seg-
ment IV. In some paratypes segments III and IV are considerably darker.
Eyes and ocelli bright yellow where not covered with dark pigment,
occellar crescents dark red. Wing membrane light brown except for a
small, clear, oval area in basal fourth.
Head nearly half again as wide as long; cheeks nearly parallel, very
slightly arched, carrying a number of pale, weak hairs; dorsum, trans-
versely striated, the striations being especially prominent posteriorly. Eyes,
prominent, slightly bulging, occupying nearly three fifths of the sides of
the head and about half of the width. Ocelli large, posterior pair lying
close to, but not touching, the inner margins of the eyes. Ocellar bristles,
large, straight, dark, and conspicuous, by far the largest on the head, (on
some paratypes 44 microns long), located well within the ocellar triangle.
Postocular bristles decidedly shorter than the ocellar, strongly curved. A
row of three small bristles on each side situated on lines drawn from the
postoculars to a point behind each posterior ocellus. A pair of small ones
anterior to the anterior ocellus.
Antennae over twice as long as the head. Segment I concolorous with
the head, segment II much darker, pedicel short and wide; sense cones on
the outer margin of segment III and the inner margin of IV large and
strongly curved. Mouth cone reaching the posterior border of the pro-


Right Antenna Head and Prothorax
Fig. 1.-Frankliniella tolucenensis sp. nov.

Head and Prothorax
Fig. 2.-Frankliniella deserti-leonum sp. nov.

Left Antenna

VOL. XXV-No. 3 45

Prothorax about as long as the head and but little wider than the head,
sharply rounded at posterior angles. Dorsum rather finely cross striated.
Spines dark and conspicuous. Anterior laterals varying in length from
20 to 30 microns, those on anterior angles from 23 to 46 microns, the
posterior one sharply recurved; those on posterior angles from 63 to 70
microns, about a dozen small bristles on dorsum, six along the anterior
margin between the anterior marginals. Metathorax much wider than the
prothorax, sides nearly parallel but often arched.
Legs rather long and slender, uniformly brown except tarsi and the
extreme bases of the hind femora which are a brownish yellow.
Wings rather short, seldom reaching tip of abdomen, anterior margin
carrying about 27 bristles, anterior vein about 21, posterior vein from
15 to 17.
Abdomen rather slender, comb on posterior margin of segment 8 com-
posed of about 12 rather long and heavy bristles. Largest bristles on
segment 8, 140 microns.
Measurements of the type: Total body length 1.37 mm.; head, length
.13 mm.; greatest width .16 mm.; prothorax, length .14 mm.; greatest
breadth .187 mm.; mesothorax width .26 mm.; abdomen, greatest width
.28 mm.; antennae length .29 mm. Length (breadth) of segments: I, 23
(28); II, 35 (28); III, 61 (23); IV, 54 (26); V, 42 (21); VI, 59 (21);
VII, 12 (9); VIII, 17 (5) microns. Ocellar bristles 44, post oculars 23.
Described from 20 females taken from the dense heads of a large
species of Eryngium growing near the top of the Volcano Nevado de Toluca,
near the city of Toluca, Mexico, altitude about 13,000 feet. Collected by the
writer on August 25, 1939. No males taken.

Frankliniella deserti-leonidum sp. nov.
FEMALE: Color by transmitted light dark brown, abdomen a blackish
brown, fore tibiae and tarsi, and antennal segments III to V, abruptly
bright yellow; wing membrane abruptly colorless in basal two fifths, shaded
with brown in apical three fifths, darker along veins. Head nearly square
in dorsal aspect but a little wider than long. Front margin nearly straight.
Dorsum crossed by two prominent nearly straight lines and some fainter
ones. Inter ocellar bristles conspicuous, each located a little inside a line
drawn through the middles of the anterior and the posterior ocelli, 23
microns long. Postocular bristles a trifle longer (28 microns) and slightly
curved, their bases very close to the posterior margins of the eyes. Cheeks
parallel but slightly arched, bearing a number of short bristles.
Antennae nearly two and a half times as long as the head. Segments
I and II brown, nearly as dark as the head, III, IV, and V abruptly light
lemon yellow, V shaded with brown in apical half, VI-VIII concolorous
with I and II, short pedicels of III-V, almost colorless, V small, narrow,
VI short and thick, abruptly rounded to a short pedicel. Sense cone on
inner angle of IV short and sharply recurved at apex; that on outer angle
of segment III longer and only slightly curved; all spines dark and con-
spicuous. Eyes large, slightly protruding, occupying a little more than
half of the sides of the head and about two thirds its width, light yellow,
rather coarsely faceted 20-30 visable in dorsal aspect; ocelli large brownish
yellow, bordered by dark red crescents, anterior directed forward, posterior


opposite the middle of the eyes and very close to their margins. Mouth
cone reaching the mesothorax.
Prothorax about as long as the head and considerably wider; sides
conspicuously arched and sharply rounded to the mesothorax. Anterior
marginal bristles 23 microns long, those at the anterior angles 31, and at
posterior angles 51 microns.
Metathorax considerably narrower than prothorax, sides nearly straight
and slightly diverging posteriorally. Legs of medium length, the hind pair
especially appear weak. Wings short and weak in comparison with the
sturdy body, not reaching the tip of the abdomen. Coastal margin with
about 21 bristles. Anterior vein with 19, posterior 14 bristles.
Abdomen heavy, much the widest part of the body. Bristles on seg-
ment IX rather short, longest 112 microns.
Measurements of type: Total body length, 1.1 mm. Head, length
.1 mm., width .114 mm.; prothorax, length .1 mm., width .18 mm.; meso-
thorax, width .22 mm.; abdomen, width .29 mm., antenna .24 mm.
Segments, length (width) : I, 21 (33) ; II, 35 (26); III, 49 (21) ; IV,
42 (23); V, 38 (18); VI, 47 (21); VII, 11 (9); VIII, 12 (7) microns.
Described from two females taken in sweeping herbs in the
"Desert-of-the-Lions." D. F. Mexico, Aug. 16, 1938. Type in
author's collection, paratype in that of Dudley Moulton, to whom
the writer is indebted for examining and criticising both of
these species.

Entomologist, State Plant Board of Florida
The following seemingly worthwhile entomological informa-
tion is taken mainly from the files of the Entomogical Depart-
ment of the State Plant Board, beginning in 1915, when the
Plant Board was organized.
In Florida Experiment Station Bulletin No. 56, 1901, Pro-
fessor H. A. Gossard, then Station Entomologist, gives an ac-
count of an outbreak of Cottony Cushion-Scale at Clearwater
(Pinellas County) in the late 90's of the last century and refers
to an unusually heavy infestation of this scale on Wax Myrtle
(Myrica cerifera). Judging from his account one would expect
to find heavy infestations of this scale on Wax Myrtle right along
as there is plenty of it growing wild in Florida and elsewhere.
However, there have been only five or six times that we have
received scale on this host indicating a paucity of infestations
on this plant. Specimens, indicating a heavier infestation, how-

VOL. XXV-No. 3

ever, have recently been received from Ridgeland, South Caro-
I have no certain explanation for the scale not occurring
more regularly and abundantly on this host plant since Gossard's
report in regard to it in 1899.
I presume one can conceive of chance variations of the scale,
one of which displayed a better liking for the Wax Myrtle at
Clearwater and developed into the extreme infestation recorded
by Gossard. Again, the variation may have occurred in the
myrtle, the myrtle in the thicket referred to by Gossard better
supplying the needs of the scale. Then, also, the soil conditions
in the thicket cannot be ruled out as these may have produced
something in the plants favoring the development of the scale.
Anyhow, the facts are as stated that the few specimens of Cot-
tony Cushion-Scale on myrtle received do not indicate heavy
infestations, except perhaps the one from South Carolina previ-
ously noted.
It would be superfluous here to give any long list of host
plants of Cottony Cushion-Scale as such has been published
elsewhere. There are, however, several other plants listed by
Gossard that have either not been found infested by the Plant
Board Inspectors or so listed by us only once or twice. Thus,
quince has been received by us only once slightly infested from
Sebring; fig only one record (slight) from West Palm Beach;
solidago goldenrodd) twice, but only slight, in Gainesville; mul-
berry and pomegranate none during the past twenty-six years.



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